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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 7-16 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We propose that crack healing in polymers occurs by the stages of surface rearrangement, surface approach, wetting, diffusion, and randomization. The stages of wetting and diffusion are responsible for the majority of the mechanical property recovery or healing, and control the intrinsic healing function Rh(t). However, the observed macroscopic recovery R is a convolution product of Rh(t) and a wetting distribution function Φ(t). Each Rh(t) function contains a wetting and diffusion component. Experiments were designed to investigate intrinsic healing functions for fracture stress, strain, and energy; the results were found to be in excellent agreement with theory.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 17 (1979), S. 385-389 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2691-2701 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Binary polymer films containing different percentages of corn starch and low-density polyethylene (LDPE) were exposed to soils over a period of 8 months and monitored for starch removal and chemical changes of the matrix using FTIR spectroscopy. A standard curve using the area of the C—O stretch band and an empirical second-degree polynomial to fit the data made it possible to calculate starch concentration over a wide range (0-46% by mass). Starch removal was found to proceed rapidly during the first 40 days and to nearcompletion in very high starch blends (52% and 67% by weight). Starch removal was slower, consisting of mostly surface removal in 29% starch blends. Weight loss data supported spectroscopic data showing similar gross features. Weight loss and spectroscopic data were consistent with percolation theory and suggested that starch removal continues past 240 days. Degradation rates in different soils containing different amounts of organic matter were approximately the same after a period of a few weeks. IR analysis did not show significant chemical changes in the polyethylene matrix after 240 days. However, the matrix did show evidence of swelling, an increase in surface area, and removal of low molecular weight components.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1575-1586 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new technique was developed to study the molecular mechanics of highly oriented polypropylene during stress relaxation and creep. The polarized infrared spectrum was recorded while the polymer was under load. Stress relaxation effects were investigated during the two-stage process of fast decay followed by a slower “dynamic equilibrium” decay by examining the stress-sensitive 975-cm-1 band and the orientation-sensitive 899-cm-1 band. In the fast decay region, the aligned chains became more highly overstressed and the nonaligned chains quickly relieved themselves of their initial overstress. These findings suggest an exchange of stress from nonaligned to aligned chain segments, without much orientation change. Also, a rupture of very highly overstressed aligned chains is though to occur. In the slow decay region, the aligned overstressed chains showed a relief of stress accompanied by some disorientation or helix distortion. Creep, however, appeared to occur via a process which involved all chains regardless of alignment. It was found that the number of highly stressed bonds increased with time at the expense of the intermediately stressed bonds. Very little change in overall orientation was noted, which probably explains the observed crazing and void formation.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 681-698 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Quantitative Fourier-transform infrared (FTIR) measurements of frequency shifts Δν and absorbance profile asymmetry are reported for various polypropylene samples as a function of uniaxial stress σ. Generally, it was found that the frequency shift coefficient αχ, defined by Δν = αχσ, depended on stress rate \documentclass{article}\pagestyle{empty}\begin{document}$\dot \sigma$\end{document}, draw ratio, λ, molecular orientation f, tensile modulus E, and annealing conditions. With annealing, αχ decreased with increasing shrinkage in the case of highly oriented isotactic PP. The αχ values for the “helix bands” were less affected than those for the “liquid bands.” With increasing \documentclass{article}\pagestyle{empty}\begin{document}$\dot \sigma$\end{document}, generally αχ increased to an apparent asymptotic limit. With increasing λ, f, or E, αχ also increased from αχ ≃ 0 for λ = 1 (spherulitic) to maximum values for highly oriented isotactic PP. The observed variations in αχ can be interpreted in terms of the changes in the peak position and shape of the nonuniform molecular stress distribution. Analogous behavior with x-ray diffraction peaks obtained for polymers under stress is discussed.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 970-977 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Craze healing was observed in many amorphous glassy polymers. A detailed study of the kinetics of craze healing in atactic polystyrene (Mw = 255,000) was conducted. The crazes were created in 0.08 mm films in air at room temperature, To, and constant stress, σo ⋍ 2,300 psi, healed at temperature Th for a time, Th, at σ = 0, and recrazed at To and σo. Nucleation times, τ1 and τ2, and growth rates, L1, and L2, for the first and second loading, respectively, were measured as a function of th and Th for individual crazes using dark field optical microscopy. Complete optical and mechanical healing was observed for Th ≥ 70°C(Tg ≅ 100°C). At constant Th, healing progressed in five stages with increasing th as follows; (i) no healing, τ2 = 0, L2 ≫ L1; (ii) partial healing, τ2 〈τ1, L2 〉 L1; (iii) similar growth, τ2 = τ1, L2 = L1; (iv) slower growth, τ2 〉 τ1, L2 〈 L1; (v) disappearance, τ2 → ∞, L2 → 0. A craze healing envelope of Th vs Th was obtained for the above stages. Craze healing occurred by line mode in which uniform healing occurred along the entire length of the craze.
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 52-57 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A lap shear joint method was used to study strength development during welding of polystyrene surfaces- The surfaces previously had not been in contact and care was taken to insure rapid wetting of the interface. The shear stress at failure, τf was measured at room temperature as a function of contact time, t, at constant welding temperatures up no 20°C above the glass transition temperature, Tg. The time dependence of welding could be well described by τfαt1/4. This result is in agreement with predictions of the reptation molecular dynamics model applied to inter-diffusion at a symmetric amorphous polymer-polymer interface. The activation energy for the thermally activated increase in strength development was determined as E = 96 kcal/mol at T = 113.5°C, which compares with E = 93,2 kcal/mole as predicted by the W-L-F theory using C1 = 13.7, C2 = 50 and Tg = 100°C. The polystyrene samples had molecular weights, Mn = 143,000 and Mw = 262.000. The time to achieve complete healing, t∞ ≍ 256 min at 118°C, was found to be of the same order of magnitude as the viscoelastic relaxation time and also with the time required for a polymer chain to diffuse a distance equal to its root mean square end-to-end vector.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 805-815 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Infrared (IR) spectroscopy was used to study molecular deformation processes in polymers as a function of stress, strain, time and temperature. Stress-induced frequency shifts were found to depend on temperature and morphology. Deformation of viscoelastic polypropylene was examined in terms of time dependent molecular stress distributions, orientation changes, conformational variations, and chain fracture. A tie chain length distribution model was used to quantitatively interpret the IR data. Molecular deformation processes of creep and stress relaxation were found to be opposite in nature, Observed long lifetimes of highly stressed chains suggest a reappraisal of existing fracture theories.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 1340-1367 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Studies of strength development at polymer-polymer interfaces are examined and applications to welding of similar and dissimilar polymers are considered. The fracture properties of the weld, namely, fracture stress, σ, fracture energy, GIc, fatigue crack propagation rate da/dN, and microscopic aspects of the deformation process are determined using compact tension, wedge cleavage, and double cantilever beam healing experiments. The mechanical properties are related to the structure of the interface via microscopic deformation mechanisms involving disentanglement and bond rupture. The time dependent structure of the welding interface is determined in terms of the molecular dynamics of the polymer chains, the chemical compatibility, and the fractal nature of diffuse interfaces. Several experimental methods are used to probe the weld structure and compare with theoretical scaling laws, Results are given for symmetric amorphous welds, incompatible and compatible asymmetric amorphous welds, incompatible semicrystalline and polymer-metal welds. The relevance of interface healing studies to thermal, friction, solvent and ultrasonic welds is discussed.
    Additional Material: 33 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 1130-1137 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The relationship of valence-coordinate deformation to the temperature dependence of some infrared peak-absorption frequencies in Poly(vinyl chloride) (PVC) and polystyrene (PS) is stated. A skeletal band and a CH2 rocking band in PVC and a ring-mode band in PS were studied in two kinds of experiments: steady heating and cooling of a quenched (nonequilibrium, glassy) sample through its glass-transition temperature, Tg, and long-term annealing of quenched samples below Tg, followed by steady heating and cooling. The results, a slope discontinuity, ΔM, in the v(T) relation at Tg and a frequency shift, Δviso, during isothermal annealing below Tg, are analyzed in two theoretical approaches. Interchain and intrachain contributions to the observed frequency shifts are expected to occur with a differing relative significance in different kinds of molecular vibrations, leading to one possible method of distinguishing valence-coordinate deformation (chain strain) from other effects.
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